Canonical Allele Identifier: CA2270105558

Gene: SMARCD2

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.63837489C= , CM000679.2:g.63837489C=	GRCh38
NC_000017.10:g.61914849C= , CM000679.1:g.61914849C=	GRCh37
NC_000017.9:g.59268581C=	NCBI36
NG_053004.1:g.10503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697953.1:n.241G=
ENST00000698016.1:c.212G=	ENSP00000513502.1:p.Arg71=
ENST00000698021.1:c.16G=
ENST00000698022.1:c.170G=	ENSP00000513504.1:p.Arg57=
ENST00000698027.1:c.212G=	ENSP00000513505.1:p.Arg71=
ENST00000448276.7:c.353G= MANE Select	ENSP00000392617.2:p.Arg118=
ENST00000225742.13:c.128G=	ENSP00000225742.9:p.Arg43=
ENST00000323347.14:c.209G=	ENSP00000318451.10:p.Arg70=
ENST00000448276.6:c.353G=	ENSP00000392617.2:p.Arg118=
ENST00000577686.1:n.53-252G=
ENST00000580054.1:c.137G=	ENSP00000463793.1:p.Arg46=
ENST00000584400.5:c.217-252G=	ENSP00000464503.1:n.217-252G=
ENST00000613943.4:c.242G=	ENSP00000483605.1:p.Arg81=
NM_001098426.1:c.353G=	NP_001091896.1:p.Arg118=
XM_005257604.2:c.128G=	XP_005257661.2:p.Arg43=
NM_001330439.1:c.128G=	NP_001317368.1:p.Arg43=
NM_001330440.1:c.209G=	NP_001317369.1:p.Arg70=
NM_001098426.2:c.353G= MANE Select	NP_001091896.1:p.Arg118=
NM_001330440.2:c.209G=	NP_001317369.1:p.Arg70=